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Revision as of 04:13, 26 October 2010 (view source) Bwpark (Talk | contribs) (→6/29/2010) ← Older edit		Revision as of 04:13, 26 October 2010 (view source) Bwpark (Talk | contribs) (→6/30/2010) Newer edit →
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	''Kevin, Marc''		''Kevin, Marc''
-	Cryopreserved stock of K12	+	Cryopreserved stock of K12:
	*1 mL located in the iGEM box in the Lin lab.		*1 mL located in the iGEM box in the Lin lab.
	*1 mL located in the lab freezer.		*1 mL located in the lab freezer.

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Revision as of 04:13, 26 October 2010

	Sunday	Monday	Tuesday	Wednesday	Thursday	Friday	Saturday
Week 1	-	6/28/2010	6/29/2010	6/30/2010	7/1/2010	-	-
Week 2	-	-	-	7/7/2010	-	-	-
Week 3	-	-	-	-	-	-	-
Week 4	-	-	-	7/21/2010	-	-	-
Week 5	-	-	7/27/2010	-	-	-	-

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6/28/2010

Kevin, Marc

Made a 500 mL batch of LB broth.

• When pouring in distilled water, pour a the powder few mL at a time to avoid clumping.
• It takes 20g of powder to make 1 L of broth.

Sterilized broth using the autoclave.

• The temperature setting on the autoclave is off by a little bit.
• Set dial 2 notches below 134°C.

6/29/2010

Kevin, Marc, Alena

Started growing E. coli K12 cultures:

• Poured 2 mL of LB broth into a Falcon tube
• Used strain of K12 from Dr. Lin's freezer
• Placed in incubator shaker for 24 hrs.

Added and inventoried supplies from Dr. Pinto's lab.

• Regular trash can be thrown out by going down one floor, then going outside to the trash bins.
• Chemical wastes must be cleaned by calling OSEH.

6/30/2010

Kevin, Marc

Cryopreserved stock of K12:

• 1 mL located in the iGEM box in the Lin lab.
• 1 mL located in the lab freezer.

7/1/2010

Kevin, Marc, Alena

Cryopreserved DH5α according to protocol procedure on 6/30/2010

• Put 1 stock in -20°C fridge in 1239
• Put the other stock in the -80°C fridge in the Lin lab

7/7/2010

Alena

Obtain genomic DNA of CFT073 E. coli strain from Dr. Mobley's Lab

• stored in -20°C fridge on ice

7/21/2010

Kevin, Marc, Alena

Met in Dude to determine sequence of fim operon. Arranged meeting with Dr. Mobley's group next Tuesday to learn more about hyperpiliation and the cloning process.

7/27/2010

Kevin, Marc, Alena

Met with Chris Alteri from Dr. Harry Mobley's research group to discuss the best route to hyperproduce the pili. Chris recommended that we create a plasmid by cloning FimB into pBAD, and then inserting that plasmid in MG1655. In theory, that should activate flocculation in the E. coli, inducible by arabinose. Chris was able to give us the procedures for creating a plasmid with FimB, as well as the procedures for knocking out a gene.

In order to test how effectively the pili flocculate, we are planning to create an E. coli strain with fimE knocked out.

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